reference/23653485

http://rdf.ncbi.nlm.nih.gov/pubchem/reference/23653485

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endingPage	1354
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publicationName	Human Mutation
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bibliographicCitation	Vahidnezhad H, Youssefian L, Saeidian AH, Touati A, Sotoudeh S, Jazayeri A, Guy A, Lovell PA, Liu L, Kariminejad A, McGrath JA, Zeinali S, Uitto J. Next generation sequencing identifies double homozygous mutations in two distinct genes (EXPH5 and COL17A1 ) in a patient with concomitant simplex and junctional epidermolysis bullosa. Human Mutation. 2018 Aug 03;39(10):1349–54. doi: 10.1002/humu.23592.
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date	2018-08-03-04:00^^<http://www.w3.org/2001/XMLSchema#date>
identifier	https://pubmed.ncbi.nlm.nih.gov/30016581 https://doi.org/10.1002/humu.23592
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language	English
source	https://pubmed.ncbi.nlm.nih.gov/ https://www.crossref.org/
title	Next generation sequencing identifies double homozygous mutations in two distinct genes (EXPH5 and COL17A1 ) in a patient with concomitant simplex and junctional epidermolysis bullosa
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